REACTIONS OF DIASTEREOMERIC AMINOBICYCLOALKYL MELDRUM ACID-DERIVATIVES - STERICALLY CONTROLLED TRANSFORMATIONS AT THE [4.1.0]-BICYCLIC SYSTEMS

被引：9

作者：

BENZING, M ^{[1
]}

VILSMAIER, E ^{[1
]}

机构：

[1] UNIV KAISERSLAUTERN,FACHBEREICH CHEM,ERWIN SCHRODINGER STR,D-6750 KAISERSLAUTERN,FED REP GER

来源：

CHEMISCHE BERICHTE-RECUEIL | 1987年 / 120卷 / 11期

关键词：

D O I：

10.1002/cber.19871201116

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1873 / 1880

页数：8

共 12 条

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[3] REACTIONS WITH AMINOBICYCLO[N.1.0]ALKANES .2. THERMOLYSIS OF AMINOBICYCLO[N.1.0]ALKANES WITH A MELDRUM ACID, A BARBITURIC-ACID, OR A THIOBARBITURIC ACID MOIETY [J].

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[5]

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[6] AN ENDO-SUBSTITUTION AT THE AMINONORCARANE SYSTEM [J].

VILSMAIER, E ;

KRISTEN, G .

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[7] ENAMINOSULFONIUM SALTS .8. ASSIGNMENT OF CONFIGURATION OF 7-AMINOBICYCLO[4.1.0]HEPTANES [J].

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[8] REACTIONS WITH AMINOBICYCLO[N.1.0]ALKANES .3. DIACYLMETHYLENECYCLOPROPANES AS INTERMEDIATES IN CYCLOPROPANE SUBSTITUTIONS [J].

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[9] ASSIGNMENT OF CONFIGURATION OF LARGER BICYCLO[N.1.0]ALKYLAMINES - THE USE OF A LANTHANIDE SHIFT-REAGENT [J].

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[10]

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